Sr. Medical Science Liaison - EMEA

Tandem Diabetes Care; United Kingdom; Hybrid; GBP 60,000 - 85,000; Full time

Job summary

A leading company in diabetes technology is seeking a Sr. Medical Sciences Liaison to strengthen relationships with the medical community and support product introduction. This hybrid role involves strategic presentations, evidence generation, and collaboration with international teams to enhance market access. Ideal candidates will have a deep understanding of diabetes management and medical device regulations, along with strong communication skills.

Benefits

Flexible working environment

Commitment to diversity and inclusion

Qualifications

• Deep scientific knowledge of diabetes disease state and clinical management.
• Demonstrated knowledge of international medical device regulations.
• Fluent in English and at least one other European language.

Responsibilities

• Develop and deliver strategic Medical Affairs presentations.
• Serve as leadership for OUS evidence generation strategy.
• Partner with in-country leaders to engage healthcare providers.

Skills

Scientific knowledge of diabetes

Technical writing

Analytical problem solving

Presentation skills

Communication with diverse groups

Education

MS, PhD, DNP, MD, PharmD or equivalent

Tools

MS Office

Adobe Acrobat

Job description

Remote - United Kingdom
111 United Kingdom
United Kingdom, 000000, GBR

Remote - United Kingdom
111 United Kingdom
United Kingdom, 000000, GBR

Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take a “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. Tandem is always looking to add talent that can help us manage our interests globally.

STAY AWESOME:

Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with -IQ technology — an advanced predictive algorithm that automates insulin delivery.

But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with type 1 diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more attandemdiabetes.com

WHEN & WHERE YOU’LL WORK:

Hybrid: This role will be a mix of in-office work and remote work.

A DAY IN THE LIFE:

The Sr. Medical Sciences Liaison liaises with the international (OUS) healthcare and scientific communities to support the market introduction and/or sustainment of the Tandem’s products, industry position, and market penetration. This role strengthens the development of the company’s relationship with the medical/scientific community by communicating product-related information to investigators and institutions and by assisting field reps and distributor partners with medical related questions which require Medical Affairs oversight. Works closely with the Medical Writer and Medical Affairs team to write up medical evidence for OUS regulatory findings and facilitate research and analyses necessary for OUS market access. Partners closely with the International Clinical Team, as well as distributor partners, industry, customers, and collaborators to address clinical questions related to the company’s current and future products.

Working as Sr. Medical Science Liaison - EMEA, you'll...

• Scientific presentations:
  • Develop and deliver strategic Medical Affairs presentations to internal and external stakeholders via webinars and in person presentations.
  • Present research studies, clinical case studies and other evidence of the safety and efficacy of Tandem products and diabetes technology landscape.
  • Translate complex medical messages to enable clear and concise understanding by both external audiences and internal stakeholders.
• Partner with in-country leaders to identify and engage with healthcare providers in the region via peer-to-peer medical information dissemination, rapport building, scientific exchange, off label discussions, and potential advisory board involvement.
• Evidence Generation:
  • Serve as leadership for OUS evidence generation strategy to identify evidence needs and disseminate information to internal and external stakeholders for the purpose of regulatory approval, commercial marketing, and premium pricing for Tandem products.
  • Monitor clinical developments, publications, and market trends, providing relevant literature reviews to ensure medical and other internal teams are kept up to date.
• Advisory Boards:
  • Partner with the global commercial organization to set up advisory boards and consulting opportunities that include region specific KOLs to gain feedback On Tandem product, evidence, and marketing strategies.
• Off label conversations:
  • Provide clinical support by responding to both on-label and off-label inquiries from medical professionals on appropriate device use, training, and indications for Tandem products, in a variety of settings.
• Support Market Access teams with information on clinical developments, publications, and market trends.
  • Assist with the integration of primary clinical and research evidence from Type 1 and Type 2 patients, clinicians, salesforce, databases, and key opinion leaders.
  • Provide internal and external scientific presentations as needed to bolster market access initiatives.
• Partner with international clinical research investigators for protocol development and execution of research studies executed OUS.
• Serve as a member of international product core teams for upstream involvement in product roll out decisions.
• Work closely with Director, Clinical Services, on the International team to coordinate clinical and medical activities for OUS Tandem regions of business.
• Work with the Medical Writer, Chief Medical Officer (CMO), and Regulatory Affairs to complete Clinical Evaluation Reports and other clinical regulatory documents to support OUS regulatory filings.
• Ensure compliance with company policies, including Privacy/HIPAA, and other legal and regulatory requirements.

WHAT YOU’LL NEED:

• Deep scientific knowledge of diabetes disease state and clinical management of type 1 and type 2 diabetes. standards of care, and diabetes technology use in diverse populations.
• Demonstrated knowledge of international medical device regulations, with specific knowledge of EU MDR and EU CE Mark.
• Excellent technical writing, editing, and proofreading skills.
• Skilled at analytical problem solving and communicating with culturally diverse groups.
• Fundamental knowledge and/or experience with statistical analyses.
• Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information.
• Skilled in developing and delivering effective presentations of scientific data and materials, including ability to effectively respond toquestions.
• Able and motivatedto work independently and as a team member with different many departments.
• Skilled at effectively communicating as aMedical Affairs expert, independent of the commercial division.
• Able to make and prioritize process and resource decisions based on overall team needs.
• Ability to plan and execute clinical and regulatory preparation activities.
• Skilled with MS Office applications as well as Adobe Acrobat.
• Fluent in English and at least one other European language (German preferred).

EXTRA AWESOME:

• MS, PhD, DNP, MD, PharmD or equivalent combination of scientific/clinical education and applicable job experience.
• 3 plusyears clinical diabetes, diabetes technology, or insulin pump industryexperience.
• Fundamental knowledge and/or experience with scientific and statistical analyses.
• Experience presenting or communicating scientific information to professional audiences.

WHY YOU’LL LOVE WORKING HERE:

At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome!

BE YOU, WITH US!

We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us.

Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone.

REFERRALS:

We love a good referral! If you know someone who would be a great fit for this position, please share!

SPONSORSHIP:

Applicants must be authorized to work for any employer in the United Kingdom. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow.